bioRxivBioinformaticsPreprint
OCD.py - Characterizing immunoglobulin inter-domain orientations
Valentin J. HoerschingeriD, Monica L. Fernández‐QuinteroiD, Franz WaibliD, Johannes KramliD, Alexander BujotzekiD, Guy J. GeorgesiD, Klaus Roman LiedliD
Abstract
SummaryInter-domain orientations between immunoglobulin domains are important for the modeling and engineering of novel antibody therapeutics. Previous tools to describe these orientations are applicable only to the variable domains of antibodies and T-cell receptors. We present the "Orientation of Cylindrical Domains (OCD)" tool, which employs a transferable approach to calculate inter-domain orientations for all immunoglobulin domains. Based on a reference structure, the OCD tool automatically builds a suitable reference coordinate system for each domain. Through alignment, the reference coordinate systems are transferred onto the sample to calculate six measures which fully characterize the inter-domain orientation. Availability and implementationThe OCD approach is implemented as a stand-alone Python script, OCD.py, which can handle multiple types of data input for the analysis of single structures and molecular dynamics trajectories alike. OCD.py is available at https://github.com/liedllab/OCD under MIT license. Supplementary InformationSupplementary information and data are available at Bioinformatics online.
- assay: protein structure
- research focus: software / tool
- approach: statistical model
- approach: experimental assay
- Citations
- 5
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- IgStrand: A universal residue numbering scheme for the Immunoglobulin-fold (Ig-fold) to study Ig-Proteomes and Ig-Interactomes
Caesar Tawfeeq, Jiyao Wang, … Philippe Youkharibache·PLoS Computational BiologyPeer-reviewed·Apr 14, 2025
- Topological and Structural Plasticity of the single Ig fold and the double Ig fold present in CD19
Philippe Youkharibache·BiomoleculesPeer-reviewed·Aug 30, 2021
- Distinct geometries, comparable interfaces: binding modes and thermodynamic implications in conventional and single domain antibodies
Antoine Hauser, Gauthier Dangla-Pélissier, Frédéric Cazals·bioRxiv·Sep 11, 2026
- A structural database of chain-chain and domain-domain interfaces of proteins
Neeladri Sen, Mallur Srivatsan Madhusudhan·Protein SciencePeer-reviewed·Aug 13, 2022
- Uncovering the flexibility of CDR loops in antibodies and TCRs through large-scale molecular dynamics
Matteo Cagiada, Fabian C. Spoendlin, … Charlotte Mary Deane·bioRxiv·Nov 10, 2025
- A penultimate classification of canonical antibody CDR conformations
S. Kelow, B. Faezov, … R. L. Dunbrack·bioRxiv·Oct 12, 2022